Human Genome Region PHF16
- Assembly:
- GRCh37.p13
- Location:
- chrX:46,609,875-47,079,810
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| KB021648.1 | NW_004166866.1 | FIX | 469,972 | 110 | 353 | |